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继发性与复发性中枢神经系统淋巴瘤:在单机构队列中评估其异同

Secondary Versus Recurrent Central Nervous System Lymphoma: Evaluating the Similarities and Differences in a Single-Institution Cohort.

作者信息

Bazer Danielle A, Schweitzer Melanie, Zabrocka Ewa, Kowalska Agnieszka

机构信息

Neurology/Neuro-Oncology, Johns Hopkins University, Baltimore, USA.

Neurology, Stony Brook University, Stony Brook, USA.

出版信息

Cureus. 2025 Jul 9;17(7):e87626. doi: 10.7759/cureus.87626. eCollection 2025 Jul.

Abstract

BACKGROUND

Primary central nervous system lymphoma (PCNSL) is a rare malignancy that affects only a small number of individuals. A subset of these cases may later relapse as recurrent central nervous system lymphoma (RPCNSL), while systemic lymphomas may progress to secondary central nervous system lymphoma (SCNSL). Although these entities differ in origin, they often present with overlapping clinical and radiologic features, complicating diagnosis and management.

OBJECTIVE

This study aims to compare the clinical presentations, treatment histories, lesion characteristics, and outcomes of patients with RPCNSL and SCNSL in a single-institution cohort in an attempt to identify key distinguishing features and shared patterns. Improved understanding of these similarities and differences may enhance diagnostic accuracy, guide treatment strategies, and inform surveillance approaches.

METHODS

We conducted a retrospective chart review of six patients (three with RPCNSL, three with SCNSL) treated at our institution between 2010 and 2020. Demographic data, initial cancer diagnosis and treatment, central nervous system (CNS) involvement, imaging findings, clinical symptoms, and outcomes were analyzed.

RESULTS

All RPCNSL lesions were solitary and localized to the frontal or temporal lobes, while SCNSL lesions were multifocal in two of three patients. Altered mental status was a common presenting symptom across both groups. Treatment regimens and timing of CNS involvement varied widely. All RPCNSL patients eventually transitioned to hospice care.

CONCLUSION

Despite differing pathogeneses, SCNSL and RPCNSL share overlapping clinical features that may obscure timely diagnosis. Recognizing their distinct patterns in lesion distribution, timing of CNS involvement, and treatment history is crucial for tailoring care and improving outcomes. Larger studies are needed to validate these findings and support the development of evidence-based guidelines.

摘要

背景

原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见的恶性肿瘤,仅影响少数个体。这些病例中的一部分可能随后复发为复发性中枢神经系统淋巴瘤(RPCNSL),而系统性淋巴瘤可能进展为继发性中枢神经系统淋巴瘤(SCNSL)。尽管这些实体起源不同,但它们通常具有重叠的临床和影像学特征,使诊断和管理变得复杂。

目的

本研究旨在比较单机构队列中RPCNSL和SCNSL患者的临床表现、治疗史、病变特征和结局,以试图识别关键的鉴别特征和共同模式。更好地理解这些异同可能会提高诊断准确性、指导治疗策略并为监测方法提供依据。

方法

我们对2010年至2020年间在本机构接受治疗的6例患者(3例RPCNSL,3例SCNSL)进行了回顾性病历审查。分析了人口统计学数据、初始癌症诊断和治疗、中枢神经系统(CNS)受累情况、影像学表现、临床症状和结局。

结果

所有RPCNSL病变均为孤立性,局限于额叶或颞叶,而3例SCNSL患者中有2例病变为多灶性。精神状态改变是两组常见的首发症状。治疗方案和CNS受累时间差异很大。所有RPCNSL患者最终都转入了临终关怀。

结论

尽管发病机制不同,但SCNSL和RPCNSL具有重叠的临床特征,可能会掩盖及时诊断。认识到它们在病变分布、CNS受累时间和治疗史方面的不同模式对于量身定制治疗和改善结局至关重要。需要更大规模的研究来验证这些发现并支持基于证据的指南的制定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2f8/12334250/2d01c003bbc2/cureus-0017-00000087626-i01.jpg

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